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カルバミルコリンクロリド

Carbachol

HCID 5831
ノート反応
基本情報概要名称と識別子物性安全と法規制化学と産業関連反応化合物ノート
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基本情報

CAS
51-83-2
標準SMILES
C[N+](C)(C)CCOC(N)=O.[Cl-]
InChIKey
AIXAANGOTKPUOY-UHFFFAOYSA-N
分子式
C6H15N2O2.Cl
平均分子量
182.65 g/mol
単同位体質量
182.0822054

概要

Prismatic crystals or powder. Odorless, but develops a faint odor of aliphatic amine upon standing in an open container. Cholinergic, parasympathomimetic, used chiefly in large animals, especially for colic in the horse. (EPA, 1998)

名称と識別子

優先名称
Carbachol
IUPAC
2-carbamoyloxyethyl(trimethyl)azanium chloride
現地名
カルバミルコリンクロリド
英語名
Carbachol
分子式
C6H15N2O2.Cl
分子量
182.65

名称と別名

carbachol51-83-2MiostatCARBACHOL CHLORIDECarbastatCarbamylcholine chlorideCarbacholineCarbacholinCarbacolinaCarbamiotinCarbocholCarbocholin
名称をさらに表示
カルバミルコリンクロリドカルバミノコリンクロリドカルバコールドリルカルボコリン[2-(アミノカルボニルオキシ)エチル]トリメチルアミニウム·クロリドレンチンモリルN,N,N-トリメチル-2-[(アミノカルボニル)オキシ]エタンアミニウム·クロリドカルバメートコリンクロリドカルバミノイルコリンクロリドカルバモイルコリンクロリドコレチルカルボコールジェストリル(2-カルバモイルオキシエチル)トリメチルアミニウム·クロリドベソペリフ2-[(アミノカルボニル)オキシ]-N,N,N-トリメチルエタンアミニウム·クロリドカルコリンカルビルCarbaCARBAMOYLCHOLINE CHLORIDEtl457
CarbocholineCarcholinVasoperifColetylLentinDorylMorylCarbacholine chloride

データベース識別子

物性

構造計算による物性

極性表面積
52.3 Ų
水素結合供与体数
1
水素結合受容体数
3
回転可能結合数
4
重原子数
11
形式電荷
0
複雑度
117

実験および物理化学的性質

pHNeutral to litmus (aqueous soln)
OdorOdorless or has a slight amine-like odor
Color/Form · 2 件

Hard prismatic crystals

White or faintly yellow crystals or crystalline powder

Solubility · 5 件

1 g in 1 ml water

1 g in 50 ml alcohol

Very slightly sol in dehydrated alcohol, more readily sol on boiling

1 g in 10 ml methanol

Practically insol in chloroform, ether, acetone

Human Drugs · 4 件

Breast Feeding; Lactation; Miotics; Muscarinic Agonists; Parasympathomimetics

FDA approved drugs -> Active ingredient

FDA approved drugs -> Active ingredient

Ophthalmological preparations > Miotics and antiglaucoma medicines

DecompositionWhen heated to decomposition it emits ... very toxic fumes of /hydrogen chloride, ammonia and nitrogen oxides/.
Melting Point · 2 件

392 to 401 °F (EPA, 1998)

200-203 °C, some decomposition

Physical DescriptionPrismatic crystals or powder. Odorless, but develops a faint odor of aliphatic amine upon standing in an open container. Cholinergic, parasympathomimetic, used chiefly in large animals, especially for colic in the horse. (EPA, 1998)

安全と法規制

安全情報は参考情報です。供給元の安全データシート(SDS)、適用法令、専門家による評価に代わるものではありません。

GHS分類

GHS Classification · 4 件

Danger

H300 (100%): Fatal if swallowed [Danger Acute toxicity, oral]

P264, P270, P301+P316, P321, P330, P405, and P501 (click each P-code to see the statement)

Aggregated GHS information provided per 72 reports by companies from 2 notifications to the ECHA C&L Inventory.

危険有害性情報

Regulatory InformationCarbamoylcholine chloride: Does not have an individual approval but may be used under an appropriate group standard
Other Safety InformationIMAP assessments - Ethanaminium, 2-[(aminocarbonyl)oxy]-N,N,N-trimethyl-, chloride: Environment tier I assessment
DOT LabelPoison
Fire HazardsWhen heated to decomposition, it emits very toxic fumes of chloride and nitrogen oxides. The aqueous solution is stable even when heated. (EPA, 1998)
Health HazardsHighly toxic by mouth. (EPA, 1998)
FDA Requirements · 2 件

Manufacturers, packers, and distributors of drug and drug products for human use are responsible for complying with the labeling, certification, and usage requirements as prescribed by the Federal Food, Drug, and Cosmetic Act, as amended (secs 201-902, 52 Stat. 1040 et seq., as amended; 21 U.S.C. 321-392).

The Approved Drug Products with Therapeutic Equivalence Evaluations List identifies currently marketed drug products, incl carbachol, approved on the basis of safety and effectiveness by FDA under sections 505 and 507 of the Federal Food, Drug, and Cosmetic Act. /From Appendix A, Product Name Index/

Reactive GroupCarbamates

化学と産業

薬理情報

ATC Code · 5 件

N07AB01

N - Nervous system

S - Sensory organs

QA - Alimentary tract and metabolism

QS - Sensory organs

Mechanism of Action · 5 件

The pharmacologic effects of all miotics are similar; they differ primarily in ocular and systemic absorption, duration of action and degree of effects. Acetylcholine, an endogenous mediator of nerve impulses, stimulates cholinergic receptors, resulting in muscarinic and nicotinic effects. The action of acetylcholine is transient. ... Pilocarpine, carbachol, and methacholine also directly stimulate cholinergic receptors; however, these drugs have a more prolonged duration of action (several hours) than does acetylcholine. There is some evidence that carbachol also has a weak anticholinesterase effect ... .

Miotics reduce intraocular pressure in normal and glaucomatous eyes. The mechanism of action of the drugs in lowering intraocular pressure has not been precisely determined. In patients with open-angle (chronic simple, noncongestive) glaucoma, the drugs facilitate aqueous humor outflow, apparently by causing contraction of the ciliary muscle and widening of the trabecular meshwork. ... Miotics decrease activity of extraocular muscles of convergence. ... Systemically absorbed miotics produce parasympathomimetic effects on various body systems. /Miotics/

/Carbachol acts/ ... with selectivity on the smooth muscle of the gastrointestinal tract ... Carbachol /also/ retains substantial nicotinic activity, particularly on autonomic ganglia. It is likely that both its peripheral and its ganglionic actions are due, in part, to the release of endogenous acetylcholine from the terminals of cholinergic fibers.

The choline esters /carbachol & bethanechol/ increase ureteral peristalsis, contract the detrusor muscle of the urinary bladder, increase the maximal voluntary voiding pressure, and decrease the capacity of the bladder. In addition, the trigone and external sphincter are relaxed. In animals with experimental lesions of the spinal cord or sacral roots, these drugs bring about satisfactory evacuation of the neurogenic bladder.

For more Mechanism of Action (Complete) data for CARBACHOL CHLORIDE (7 total), please visit the HSDB record page.

Metabolism/Metabolites · 1 件

Carbachol, which is an unsubstituted carbamyl ester, is totally resistant to hydrolysis by either acetylcholinesterase or nonspecific cholinesterases; its half-life is thus sufficiently long that it is distributed to areas of low blood flow.

関連反応

0 件
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化合物ノート

読み込み中…

このページの内容基本情報概要名称と識別子物性安全と法規制化学と産業関連反応化合物ノート
CAS
51-83-2
PubChem CID
5831
DTXSID
DTXSID9022730
ChEMBL
CHEMBL14
ChEBI
CHEBI:3385
UNII
8Y164V895Y
EC Number
200-127-3
Stability/Shelf LifeThe aqueous soln is stable even when heated.
Collision Cross Section128 Ų [M+H]+ [CCS Type: TW; Method: calibrated with polyalanine and drug standards]
Other Experimental Properties · 4 件

Hygroscopic

Ophthalmic soln of carbachol has a pH of 5-7; the commercially available intraocular injection has a pH of 6.5-7.5 /Soln/

Chlorocresol (0.025 to 0.1%) and chlorbutol (0.5%) were incompatible with a soln of carbachol (0.8%) and sodium chloride (0.69%), very slight precipitates forming on heating and increasing on standing. /Soln/

Incompatible with alkalies, iodine, and silver salts

物理化学的性質

融点
210 °C · 210 °C (dec.) (lit.)
比重(密度)
1.2798 · 1.2798 (rough estimate)
屈折率
1.5557 · 1.5557 (estimate)
貯蔵温度
Desiccate at RT
溶解性
2 O: · H2O: 1 g/mL
外見
結晶性
酸解離定数(Pka)
4.8 · pKa 4.8 (Uncertain)
色
白い
水溶解度
1 · 1.0グラム/ミリリットル
Merck
14 · 14,1779
BRN
3917459 · 3917459
安定性
Hygroscopic
InChI
1S/C6H14N2O2.ClH/c1-8(2,3)4-5-10-6(7)9;/h4-5H2,1-3H3,(H-,7,9);1H
InChIKey
AIXAANGOTKPUOY-UHFFFAOYSA-N
SMILES
[Cl-].C[N+](C)(C)CCOC(N)=O
CAS データベース
51 · 51-83-2(CAS DataBase Reference)
NISTの化学物質情報
Carbachol(51-83-2)
EPAの化学物質情報
Carbachol chloride (51-83-2)

化学的性質

化学的特性Carbachol chloride is a crystalline odorless powder which, on standing in an open container, develops a faint odor resembling that of an aliphatic amine.

Reactivity Profile · 1 件

CARBACHOL CHLORIDE is a carbamate ester. Carbamates are chemically similar to, but more reactive than amides. Like amides they form polymers such as polyurethane resins. Carbamates are incompatible with strong acids and bases, and especially incompatible with strong reducing agents such as hydrides. Flammable gaseous hydrogen is produced by the combination of active metals or nitrides with carbamates. Strongly oxidizing acids, peroxides, and hydroperoxides are incompatible with carbamates.

Air and Water ReactionsHygroscopic.
CERCLA Reportable Quantities · 1 件

Releases of CERCLA hazardous substances are subject to the release reporting requirement of CERCLA section 103, codified at 40 CFR part 302, in addition to the requirements of 40 CFR part 355. Carbachol chloride is an extremely hazardous substance (EHS) subject to reporting requirements when stored in amounts in excess of its threshold planning quantity (TPQ) of 500/10,000 lbs.

Hazard Classes and CategoriesAcute Tox. 2 (100%)

安全と保護具

Fire FightingExcerpt from ERG Guide 154 [Substances - Toxic and/or Corrosive (Non-Combustible)]:
First AidNote: Carbachol chloride is a direct cholinergic agonist. Due to spontaneous vomiting, administration of syrup of Ipecac is unnecessary. Cathartics will usually not be needed.
Storage Conditions · 2 件

Store in airtight containers. Protect from light.

Aqueous solutions are most stable to autoclaving when buffered to pH 3.5. Up to 5% decomposition may occur when unbuffered solutions are heated in an autoclave, and the decomposition increases the pH of the solutions; such autoclaved solutions should not be stored for more than a yr.

Nonfire Spill ResponseAvoid skin contact. (EPA, 1998)
Isolation and EvacuationExcerpt from ERG Guide 154 [Substances - Toxic and/or Corrosive (Non-Combustible)]:
Protective Action Criteria (PAC) · 3 件

1.4 [mg/m3]

15 [mg/m3]

90 [mg/m3]

Personal Protective Equipment (PPE) · 1 件

For emergency situations, wear a positive pressure, pressure-demand, full facepiece self-contained breathing apparatus (SCBA) or pressure- demand supplied air respirator with escape SCBA and a fully-encapsulating, chemical resistant suit. (EPA, 1998)

毒性情報

Interactions · 5 件

Acetylcholine and methacholine are hydrolyzed by acetylcholinesterase and their effects are markedly enhanced by the prior administration of anticholinesterase agents. The latter drugs produce only additive effects with the stable analogs, carbachol and bethanechol. The muscarinic actions of all the drugs of this class are blocked selectively by atropine, through competitive occupation of cholinergic receptor sites on the autonomic effector cells and on the secondary muscarinic receptors of autonomic ganglion cells.

When used in conjunction with topical epinephrine, topical timolol, and/or systemically admin carbonic anhydrase inhibitiors, the effect of miotics in lowering intraocular pressure may be additive. /Miotics/

Although the clinical importance has not been established, the miotic and/or ocular hypotensive effects of miotics reportedly may be antagonized by long-term topical or systemic corticosteroid therapy, systemic anticholinergics, antihistamines, meperidine, sympathomimetics, & tricyclic antidepressants ... .

Ophthalmic carbachol may be ineffective when administred following ophthalmic flubiprofen; the pharmacologic basis for this interference is not known.

Concurrent use of ... /ophthalmic belladona alkaloids or cyclopentolate/ may interfere with the antiglucoma action of carbachol; also concurrent use with carbachol counteracts the myrdiatic effects of these medications ... .

Human Toxicity Excerpts · 5 件

Systemic reactions after chronic topical application of /some/ ... miotics to the eye or intraocular injection of acetylcholine or carbachol are rare and usually occur only with very frequent admin. ... Adverse systemic effects of miotics result from parasympathetic stimulation and the most common effects, especially in children, include nausea, vomiting, diarrhea, abdominal pain, and intestinal cramps.

A 58-yr-old man developed esophageal rupture 2 hr after a subcutaneous injection of carbachol to relieve urinary retention.

A report of life-threatening attacks of profuse sweating, intestinal cramps ... defecation, hypothermia, hypotension, and bradycardia in a 36-yr-old man due to carbachol intoxication /was recorded/. A 10-yr-old boy had died following similar attacks associated with repeated carbachol ingestion.

The most common ... effects of miotic therapy are painful ciliary or accommodative spasm, blurred vision or myopia, and poor vision in dim light. ... Other adverse effects ... include ciliary or conjunctival congestion, lacrimal passage stenosis, twitching of the eyelids, stinging, burning, lacrimation, ocular or brow pain, headache, photophobia ... /Miotics/

Tests of 0.01% solution introduced into the anterior chamber of eyes of human beings ... have shown no significant irritating or injurious action, but prompt miotic effect.

Non-Human Toxicity Excerpts · 4 件

Carbachol, in doses sufficient to cause purgation /in animals/, produces a profound drop in the diastolic blood pressure. Larger doses aggravate this by inhibiting the heart itself.

All parasympathomimetic drugs, in toxic doses, stimulate all the secretions and produce severe gastrointestinal colic and diarrhea and dyspnea; the iris is markedly constricted; the heart rate is first increased and then slowed. Death may be due to respiratory paralysis or heart block. /Parasympathomimetic drugs/

The phenomenon of sudden mortality in the chick embryo, induced by the exogenous neurotransmitter /such as/ carbachol, is described. When introduced singly into eggs (albumen) in doses of 0.1 mg/egg, /the cmpd/ induced highly significant, sharply incr mortality (60-100%) when the introduction was on embryonic (incubation) days 8 to 12, but none if introduction was earlier. These ages follow the appearance of functional receptors (or receptor-effectors) for the substance. ... The involvement of receptors here have not been proved. Solvent alone (Ringer's solution for chick) had no effect, indicating that the procedures used were in themselves not lethal. ...

Tests of 0.01% solution intrduced into the anterior chamber of eyes of rabbits, cats ... have shown no significant irritating or injurious action, but prompt miotic effect.

Antidote and Emergency TreatmentAtropine sulfate injection is used as an antidote to the systemic effects of carbachol.
Effects During Pregnancy and Lactation◉ Summary of Use during Lactation
Non-Human Toxicity Values · 2 件

LD50 Mouse oral 5 mg/kg

LD50 Mouse iv 0.3 mg/kg

法規制情報

FDA Requirements · 2 件

Manufacturers, packers, and distributors of drug and drug products for human use are responsible for complying with the labeling, certification, and usage requirements as prescribed by the Federal Food, Drug, and Cosmetic Act, as amended (secs 201-902, 52 Stat. 1040 et seq., as amended; 21 U.S.C. 321-392).

The Approved Drug Products with Therapeutic Equivalence Evaluations List identifies currently marketed drug products, incl carbachol, approved on the basis of safety and effectiveness by FDA under sections 505 and 507 of the Federal Food, Drug, and Cosmetic Act. /From Appendix A, Product Name Index/

CERCLA Reportable Quantities · 1 件

Releases of CERCLA hazardous substances are subject to the release reporting requirement of CERCLA section 103, codified at 40 CFR part 302, in addition to the requirements of 40 CFR part 355. Carbachol chloride is an extremely hazardous substance (EHS) subject to reporting requirements when stored in amounts in excess of its threshold planning quantity (TPQ) of 500/10,000 lbs.

安全データ

wgk
3
tsca
TSCA listed
rtecs
GA0875000
ridadr
UN 2811 6.1/PG 2
毒性
LD50 in mice (mg/kg): 15 orally, 0.3 i.v. (Molitor)
hs_code
29239000
risk_code
25-36/37/38
hazard_code
T
safety_code
45-36/37/39-28A-26
hazard_class
6.1
packing_group
II
Hazard Classifications
Acute Tox. 2 Oral
ストレージクラス
6.1A - Combustible acute toxic Cat. 1 and 2very toxic hazardous materials
有毒物質データの
51-83-2(Hazardous Substances Data)
FDA Pharmacological Classification · 2 件

CARBACHOL

Cholinergic Receptor Agonist [EPC]; Cholinergic Agonists [MoA]

MeSH Pharmacological Classification · 4 件

Agents that have a strengthening effect on the heart or that can increase cardiac output. They may be CARDIAC GLYCOSIDES; SYMPATHOMIMETICS; or other drugs. They are used after MYOCARDIAL INFARCT; CARDIAC SURGICAL PROCEDURES; in SHOCK; or in congestive heart failure (HEART FAILURE).

Agents causing contraction of the pupil of the eye. Some sources use the term miotics only for the parasympathomimetics but any drug used to induce miosis is included here.

Drugs that bind to and activate cholinergic receptors.

A subclass of analgesic agents that typically do not bind to OPIOID RECEPTORS and are not addictive. Many non-narcotic analgesics are offered as NONPRESCRIPTION DRUGS.

Absorption, Distribution and ExcretionTopical carbachol penetrates intact corneal epithelium very poorly; combination with wetting agent ... greatly improves corneal penetration by the drug. ... Carbachol /is/ ... absorbed through intact skin.

用途と製造

Uses · 2 件

MEDICATION (VET)

MEDICATION

Methods of ManufacturingPrepared by the interaction of beta-chloroethylcarbamate and trimethylamine.
Formulations/Preparations · 3 件

Commercially available ophthalmic solutions contain benzalkonium chloride as preservative and wetting agent. ... Preparations: Ophthalmic - Injection, for intraocular use only 100 ug/ml (0.01%) Miostat Intraocular. Solution: 0.75%, Isopto Carbachol (with benzalkonium chloride; viscous); 1.5%, Isopto Carbachol (with benzalkonium chloride; viscous); 2.25%, Isopto (with benzalkonium chloride: viscous); 3% Isotop Carbachol (with benzalkomum chloride; viscous).

Eyedrops: APF has carbachol 750 mg, sodium chloride 700 mg, benzalkonium chloride soln 0.02 ml, disodium edetate 50 mg. Water for injections to 100 ml ... Another formula: carbachol 800 mg, anhydrous dextrose 5 g, chlorhexidine acetate 5 mg. Water for injection to 100 ml ...

Carbachol intraocular soln is a sterile soln of carbachol in an aqueous medium. It contains not less than 90.0% & not more than 115.0% of the labeled amt of Carbachol. It contains no preservatives or antimicrobial agents.

General Manufacturing InformationEthanaminium, 2-[(aminocarbonyl)oxy]-N,N,N-trimethyl-, chloride (1:1): ACTIVE
応用分野 · 5 件

用途医薬品原料。

説明Unlike acetylcholine and methacholine, carbachol contains a carbamino functional group instead of an acetyl group, which is not responsive to hydrolysis by cholinesterase. In vitro studies have shown that the rate of hydrolysis is at least twice as slow as that of acetylcholine.

使用Carbachol is a powerful cholinic ester that stimulates both muscarinic and nicotinic receptors, as well as exhibits all of the pharmacological properties of acetylcholine while in addition resulting in vasodilation, a decrease in heart rate, an increase in tone and contractability of smooth muscle, stimulation of salivary, ocular, and sweat glands as well as autonomic ganglia and skeletal muscle. For this reason, use of carbachol, like acetylcholine, is limited. The exception is that it is used in ophthalmological practice and postoperational intestines and bladder atony. Upon administration in the eye, the pupil constricts and the intraocular pressure is reduced. It is used for severe chronic glaucoma.

使用Carbachol is a cholinergic agonist and is used for the treatment of glaucoma. It is also used as ophthalmic solution (eye drops) during ophthalmic surgery.

一般的な説明Carbachol forms a carbamylester in the active site of AChE, which is hydrolyzedmore slowly than an acetyl ester. This slower hydrolysis ratereduces the amount of free enzyme and prolongs the durationof ACh in the synapse. Carbachol also stimulates theautonomic ganglia and causes contraction of skeletal musclebut differs from a true muscarinic agent in that it does nothave cardiovascular activity despite the fact that it seems toaffect M2 receptors.

上流・下流製品情報

上流原料

尿素2-クロロエタノールコリン クロリドトリメチルアミン水溶液 3 0 %塩化カルボニル

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補足説明

定義An acetylcholine counterfit molecule that is not inactivated by acetylcholinesterase and is a slowly hydrolyzed cholinergic agonist that acts at both muscarinic and nicotinic receptors.